Pressure-induced polymerization of charged triple-bond monomers like acetylide and cyanide could lead to formation of a conductive metal-carbon network composite, thus providing a new route to synthesize inorganic/organic conductors with tunable composition and properties. The industry application of this promising synthetic method is mainly limited by the reaction pressure needed, which is often too high to be reached for gram amounts of sample. Here we successfully synthesized highly conductive Li3Fe(CN)6 at maximum pressure around 5 GPa and used in situ diagnostic tools to follow the structural and functional transformations of the sample, including in situ X-ray and neutron diffraction and Raman and impedance spectroscopy, along with the neutron pair distribution function measurement on the recovered sample. The cyanide anions start to react around 1 GPa and bond to each other irreversibly at around 5 GPa, which are the lowest reaction pressures in all known metal cyanides and within the technologically achievable pressure range for industrial production. The conductivity of the polymer is above 10(-3) S · cm(-1), which reaches the range of conductive polymers. This investigation suggests that the pressure-induced polymerization route is practicable for synthesizing some types of functional conductive materials for industrial use, and further research like doping and heating can hence be motivated to synthesize novel materials under lower pressure and with better performances.
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http://dx.doi.org/10.1021/acs.inorgchem.5b01851 | DOI Listing |
Nano Lett
January 2025
Center for High Pressure Science and Technology Advanced Research, Beijing 100193, P. R. China.
Saturated sp-carbon nanothreads (CNTh) have garnered significant interest due to their predicted high Young's modulus and thermal conductivity. While the incorporation of heteroatoms into the central ring has been shown to influence the formation of CNTh and yield chemically homogeneous products, the impact of pendant groups on the polymerization process remains underexplored. In this study, we investigate the pressure-induced polymerization of phenol, revealing two phase transitions occurring below 0.
View Article and Find Full Text PDFPhys Chem Chem Phys
January 2025
Center for High Pressure Science and Technology Advanced Research, Beijing 100193, P. R. China.
Pressure-induced polymerization (PIP) of aromatic molecules has emerged as an effective method for synthesizing various carbon-based materials. The selection of suitable functionalized molecular precursors is crucial for obtaining the desired structures and functions. In this work, 1,4-difluorobenzene (1,4-DFB) was selected as the building block for PIP.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
December 2024
Center for High Pressure Science and Technology Advanced Research, Shanghai 201203, China.
High pressure can create extreme conditions that enable the formation of novel materials and the discovery of new phenomena. However, the ability to preserve the desirable characteristics of materials obtained under high pressure has remained an elusive challenge, as the pressure-induced changes are typically reversible, except for the pressure-induced chemical reactions such as polymerization of hydrocarbons. Here, we propose the concept of "pressure aging" (PA) that enables the permanent locking-in of high-pressure structures and their associated enhanced properties in functional materials.
View Article and Find Full Text PDFMacromol Rapid Commun
December 2024
Faculty of Physics, Adam Mickiewicz University, Uniwersytetu Poznanskiego 2, Poznan, 61-614, Poland.
Polymer colloidal crystals (PCCs) have been widely explored as acoustic and optical metamaterials and as templates for nanolithography. However, fabrication impurities and fragility of the self-assembled structures are critical bottlenecks for the device's efficiency and applications. We have demonstrated that temperature-assisted pressure [ annealing results in the mechanical strengthening of PCCs, which improves with the annealing temperature.
View Article and Find Full Text PDFFood Chem
February 2025
College of Food Science, Fujian Agriculture and Forestry University, Fuzhou 350002, China; Fujian Provincial Key Laboratory of Quality Science and Processing Technology in Special Starch, Fujian Agriculture and Forestry University, Fuzhou 350002, China; China-Ireland International Cooperation Centre for Food Material Science and Structure Design, Fujian Agriculture and Forestry University, Fuzhou 350002, China. Electronic address:
Pressure promotes the formation of starch-polyphenol complexes, but their classification and properties are still unclear. This study aimed to elucidate the effects of dynamic high-pressure homogenization (10-50 MPa) and static hydrostatic pressure (100-500 MPa) on the copolymerization behavior and properties of lotus seed starch (LS)-endogenous polyphenol chlorogenic acid (CA) complexes. The results showed that both pressures induced LS-CA to form stable inclusion-type complexes and easily destructible noninclusion-type complexes.
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